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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112738copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,619-3,951,208 , GRCh38.p12 chr6: 149,619-3,950,974 LINC01600, TUBB2BP1, 66 more genes
    nsv5369157translocation1nstd200human GRCh38 chr6: 3,454,828-3,454,828 , GRCh38 chr6: 3,454,921-3,454,921 , GRCh37.p13 chr6: 3,455,062-3,455,062 , GRCh37.p13 chr6: 3,455,155-3,455,155 LOC643327, SLC22A23
    nsv5341585translocation1nstd200human GRCh37 chr6: 3,455,155-3,455,155 , GRCh37 chr6: 3,455,062-3,455,062 , GRCh38.p12 chr6: 3,454,828-3,454,828 , GRCh38.p12 chr6: 3,454,921-3,454,921 SLC22A23, LOC643327
    nsv4675171copy number variation1nstd102humanUncertain significance GRCh37 chr6: 3,409,111-3,734,008 , GRCh38.p12 chr6: 3,408,877-3,733,774 LOC643327, PXDC1, 4 more genes
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4118191copy number variation1nstd166human GRCh37.p13 chr6: 3,463,630-3,468,424 , GRCh38.p12 chr6: 3,463,396-3,468,190 LOC643327
    nsv4117491copy number variation1nstd166human GRCh37.p13 chr6: 3,456,589-3,457,463 , GRCh38.p12 chr6: 3,456,355-3,457,229 SLC22A23, LOC643327
    nsv3923249copy number variation1nstd102humanPathogenic NCBI36 chr6: 110,675-8,981,266 , GRCh38 chr6: 165,675-9,036,034 , GRCh37 chr6: 165,675-9,036,267 LOC100506207, LOC105374889, 148 more genes
    nsv3923206copy number variation1nstd102humanPathogenic NCBI36 chr6: 108,083-3,404,840 , GRCh38 chr6: 163,083-3,459,607 , GRCh37 chr6: 163,083-3,459,841 LOC105374883, MIR4645, 58 more genes
    nsv3922576copy number variation1nstd102humanPathogenic GRCh37 chr6: 164,633-6,284,470 , GRCh38 chr6: 164,633-6,284,237 , NCBI36 chr6: 109,633-6,229,469 GLRX3P2, CDYL, 106 more genes
    nsv3922052copy number variation1nstd102humanPathogenic GRCh37 chr6: 155,807-17,058,645 , NCBI36 chr6: 100,807-17,166,624 , GRCh38 chr6: 155,807-17,058,414 ECI2-DT, RNU1-11P, 268 more genes
    nsv3921817copy number variation1nstd102humanPathogenic GRCh37 chr6: 2,862,874-16,698,019 , GRCh38 chr6: 2,862,640-16,697,788 , NCBI36 chr6: 2,807,873-16,805,998 RN7SKP293, LOC105374906, 230 more genes
    nsv3921201copy number variation1nstd102humanUncertain significance NCBI36 chr6: 101,974-4,892,090 , GRCh37 chr6: 156,974-4,947,091 , GRCh38 chr6: 156,974-4,946,857 LOC100422781, RN7SL352P, 86 more genes
    nsv3921027copy number variation1nstd102humanPathogenic GRCh38 chr6: 389,423-13,474,956 , GRCh37 chr6: 389,423-13,475,188 , NCBI36 chr6: 334,423-13,583,167 LOC105374898, HIVEP1, 215 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
    nsv3920236copy number variation1nstd102humanPathogenic GRCh37 chr6: 164,633-5,823,834 , GRCh38 chr6: 164,633-5,823,601 , NCBI36 chr6: 109,633-5,768,833 TUBB2A, SERPINB9-AS1, 98 more genes
    nsv3918645copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 101,974-11,659,036 , GRCh37 chr6: 156,974-11,551,050 , GRCh38 chr6: 156,974-11,550,817 BMP6, BPHL, 194 more genes
    nsv3917576copy number variation1nstd102humanPathogenic GRCh38 chr6: 144,957-5,239,181 , NCBI36 chr6: 89,957-5,184,413 , GRCh37 chr6: 144,957-5,239,414 MIR3691, PRPF4B, 94 more genes
    nsv3916436copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-7,122,992 , NCBI36 chr6: 101,974-7,067,991 , GRCh38 chr6: 156,974-7,122,759 LINC01011, FOXF2, 119 more genes
    nsv3916403copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-4,907,692 , GRCh37 chr6: 156,974-4,907,926 , NCBI36 chr6: 101,974-4,852,925 MIR6720, LOC643327, 86 more genes
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